The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125199291 12519929 1 I 20160615 20160623 20160701 20160701 EXP CO-ALEXION PHARMACEUTICALS INC-A201604804 ALEXION 27.72 YR F Y 0.00000 20160701 CN CO CO

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125199291 12519929 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
125199291 12519929 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W AE1235B05 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125199291 12519929 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
125199291 12519929 OT
125199291 12519929 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125199291 12519929 Asthenia
125199291 12519929 Fatigue
125199291 12519929 Haemoglobin decreased
125199291 12519929 Haemoglobinuria
125199291 12519929 Haemolysis
125199291 12519929 Jaundice

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125199291 12519929 1 20120412 20120503 0
125199291 12519929 2 20120515 0